Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18670 | A08 | 14909249 | C | T | missense_variant | MODERATE | c.1027G>A|p.Glu343Lys |
S283 |
2 | BAA08g18670 | A08 | 14909762 | C | T | intron_variant | MODIFIER | c.749-26G>A| |
S74 |
3 | BAA08g18670 | A08 | 14910054 | C | T | missense_variant | MODERATE | c.571G>A|p.Glu191Lys |
S143 |
4 | BAA08g18670 | A08 | 14910939 | C | T | intron_variant | MODIFIER | c.427-650G>A| |
S59 |
5 | BAA08g18670 | A08 | 14911712 | C | T | intron_variant | MODIFIER | c.426+1133G>A| |
S250 |
6 | BAA08g18670 | A08 | 14911987 | G | A | intron_variant | MODIFIER | c.426+858C>T| |
S61 |
7 | BAA08g18670 | A08 | 14912093 | C | T | intron_variant | MODIFIER | c.426+752G>A| |
S240 |
8 | BAA08g18670 | A08 | 14912496 | C | T | intron_variant | MODIFIER | c.426+349G>A| |
S139 |
9 | BAA08g18670 | A08 | 14913051 | C | T | missense_variant | MODERATE | c.220G>A|p.Asp74Asn |
S299 |
10 | BAA08g18670 | A08 | 14913126 | A | T | missense_variant | MODERATE | c.199T>A|p.Ser67Thr |
S207 |
11 | BAA08g18670 | A08 | 14913175 | C | T | synonymous_variant | LOW | c.150G>A|p.Lys50Lys |
S181 |
12 | BAA08g18670 | A08 | 14915423 | C | T | upstream_gene_variant | MODIFIER | c.-1905G>A| |
S1 S90 |
13 | BAA08g18670 | A08 | 14916043 | C | T | upstream_gene_variant | MODIFIER | c.-2525G>A| |
S276 |
14 | BAA08g18670 | A08 | 14916238 | C | T | upstream_gene_variant | MODIFIER | c.-2720G>A| |
S166 |